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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-1034
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-69
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6818
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 2007-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1793c5ae21d0ab4d88ac1597dfeda03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_424686047e50c8942a815274aed8edf3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4dd7f02c38491020ab7060d72e857845
publicationDate 2009-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101454672-A
titleOfInvention Method for genetic selection of high-plasmid producing e. coli clones
abstract The present invention relates to methods of selecting for highly productive clones of E. coli for the production of plasmid DNA comprising measuring the frequency of IS1 transposon insertional mutagenesis within either the plasmid or genomic DNA of transformed clonal subtypes. An increase in IS1 insertional mutagenesis is correlated with clonal subtypes likely to exhibit a low specific productivity. The PCR-based, genetic selection assays disclosed herein are amenable to high throughput analysis, reducing the time to identify highly productive clones capable of cultivating large quantities of plasmid DNA on an industrial scale.
priorityDate 2006-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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